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University Medical Center Groningen
Department of Genetics -
L1CAM Mutation Database
Introduction
Database
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Mutations
Protein domains
References
Mutation Details
DNA change
Protein change
Exon/intron
Type
Reported classification
Bateman
SIFT
PolyPhen
Conserved
Protein domain
Remarks
LOVD ID
c.1963A>G
p.Lys655Glu
Exon 16
Missense
Disease-causing
Surface site
Tolerated
Benign
Moderately
Fn 1
Patients
Family
# Affected relatives
Clinical features
Remarks
Reference
1
unknown
Hydrocephalus, ?
Izumoto et al. (1996)
References
Year
Author
Title
Journal
Volume
Pages
Weblink
2002
De Angelis et al.
Disease-associated mutations in L1 CAM interfere with ligand interactions and cell-surface expression
Hum. Mol. Genet.
11
1-12
11772994
1996
Izumoto et al.
A new mutation of the L1CAM gene in an X-linked hydrocephalus family
Child's Nerv Syst
12
742-747
9118141
2000
Kenwrick et al.
Neural cell recognition molecule L1: relating biological complexity to human disease mutations
Hum. Mol. Genet.
9
879-886
10767310